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Webinar Overview
Viral clearance (VC) is just as critical for medical devices as it is for drugs in helping to ensure products are free from potential viruses. In this webinar our experts will provide key strategies you can apply to your own medical device viral clearance program, including study guidelines, the types of materials and model viruses used, and methods for performing VC testing on solid materials.
View this webinar to learn:
- Why viral clearance testing of medical devices is critical for compliance and safety
- How testing strategies, including the choice of materials and model viruses, can impact study effectiveness
- How to anticipate and avoid regulatory hurdles
A case study will also be presented where you will gain insights on how to overcome challenges including tight dose ranges and regulatory complexities.
Webinar Presenters
Tareq Jaber, PhD
Associate Director, Process Evaluation
Charles River
Sandra Zucchet, MSc
Viral Clearance R&D Scientist, Biologics Testing Solutions
Charles River
Carly Jurimas, MS
Principal Engineer, Microbiology and Product Biosafety
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